Factors Influencing Atypical Clinical Presentations during the 2017 Madagascar Pneumonic Plague Outbreak: A Prospective Cohort Study

In late 2017, Madagascar experienced a large urban outbreak of pneumonic plague, the largest outbreak to date this century. During the outbreak, there were widespread reports of plague patients presenting with atypical symptoms, such as prolonged duration of illness and upper respiratory tract sympt...

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Published inThe American journal of tropical medicine and hygiene Vol. 102; no. 6; pp. 1309 - 1315
Main Authors Salam, Alex P., Raberahona, Mihaja, Andriantsalama, Prisca, Read, Liam, Andrianarintsiferantsoa, Faraniaina, Razafinambinintsoa, Tiana, Rakotomalala, Rado, Hasiniatsy, Rodrigue N. E., Razafimandimby, Dominique, Castle, Lyndsey, Funk, Anna, Mangahasimbola, Reziky T., Renaud, Bertrand, Bertherat, Eric, Lovering, Andrew, Heraud, Jean-Michel, Andrianaivoarimanana, Voahangy, Frédérique, Randrianirina, Razanajatovo, Norosoa, Baril, Laurence, Fontanet, Arnaud, Rajerison, Minoarisoa, Horby, Peter, Randria, Mamy, Randremanana, Rindra
Format Journal Article
LanguageEnglish
Published United States Institute of Tropical Medicine 01.06.2020
American Society of Tropical Medicine and Hygiene
The American Society of Tropical Medicine and Hygiene
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Abstract In late 2017, Madagascar experienced a large urban outbreak of pneumonic plague, the largest outbreak to date this century. During the outbreak, there were widespread reports of plague patients presenting with atypical symptoms, such as prolonged duration of illness and upper respiratory tract symptoms. Reported mortality among plague cases was also substantially lower than that reported in the literature (25% versus 50% in treated patients). A prospective multicenter observational study was carried out to investigate potential reasons for these atypical presentations. Few subjects among our cohort had confirmed or probable plague, suggesting that, in part, there was overdiagnosis of plague cases by clinicians. However, 35% subjects reported using an antibiotic with anti-plague activity before hospital admission, whereas 55% had antibiotics with anti-plague activity detected in their serum at admission. Although there may have been overdiagnosis of plague by clinicians during the outbreak, the high frequency of community antibiotic may partly explain the relatively few culture-positive sputum samples during the outbreak. Community antibiotic use may have also altered the clinical presentation of plague patients. These issues make accurate detection of patients and the development of clinical case definitions and triage algorithms in urban pneumonic plague outbreaks difficult.
AbstractList In late 2017, Madagascar experienced a large urban outbreak of pneumonic plague, the largest outbreak to date this century. During the outbreak, there were widespread reports of plague patients presenting with atypical symptoms, such as prolonged duration of illness and upper respiratory tract symptoms. Reported mortality among plague cases was also substantially lower than that reported in the literature (25% versus 50% in treated patients). A prospective multicenter observational study was carried out to investigate potential reasons for these atypical presentations. Few subjects among our cohort had confirmed or probable plague, suggesting that, in part, there was overdiagnosis of plague cases by clinicians. However, 35% subjects reported using an antibiotic with anti-plague activity before hospital admission, whereas 55% had antibiotics with anti-plague activity detected in their serum at admission. Although there may have been overdiagnosis of plague by clinicians during the outbreak, the high frequency of community antibiotic may partly explain the relatively few culture-positive sputum samples during the outbreak. Community antibiotic use may have also altered the clinical presentation of plague patients. These issues make accurate detection of patients and the development of clinical case definitions and triage algorithms in urban pneumonic plague outbreaks difficult.
In late 2017, Madagascar experienced a large urban outbreak of pneumonic plague, the largest outbreak to date this century. During the outbreak, there were widespread reports of plague patients presenting with atypical symptoms, such as prolonged duration of illness and upper respiratory tract symptoms. Reported mortality among plague cases was also substantially lower than that reported in the literature (25% versus 50% in treated patients). A prospective multicenter observational study was carried out to investigate potential reasons for these atypical presentations. Few subjects among our cohort had confirmed or probable plague, suggesting that, in part, there was overdiagnosis of plague cases by clinicians. However, 35% subjects reported using an antibiotic with anti-plague activity before hospital admission, whereas 55% had antibiotics with anti-plague activity detected in their serum at admission. Although there may have been overdiagnosis of plague by clinicians during the outbreak, the high frequency of community antibiotic may partly explain the relatively few culture-positive sputum samples during the outbreak. Community antibiotic use may have also altered the clinical presentation of plague patients. These issues make accurate detection of patients and the development of clinical case definitions and triage algorithms in urban pneumonic plague outbreaks difficult.In late 2017, Madagascar experienced a large urban outbreak of pneumonic plague, the largest outbreak to date this century. During the outbreak, there were widespread reports of plague patients presenting with atypical symptoms, such as prolonged duration of illness and upper respiratory tract symptoms. Reported mortality among plague cases was also substantially lower than that reported in the literature (25% versus 50% in treated patients). A prospective multicenter observational study was carried out to investigate potential reasons for these atypical presentations. Few subjects among our cohort had confirmed or probable plague, suggesting that, in part, there was overdiagnosis of plague cases by clinicians. However, 35% subjects reported using an antibiotic with anti-plague activity before hospital admission, whereas 55% had antibiotics with anti-plague activity detected in their serum at admission. Although there may have been overdiagnosis of plague by clinicians during the outbreak, the high frequency of community antibiotic may partly explain the relatively few culture-positive sputum samples during the outbreak. Community antibiotic use may have also altered the clinical presentation of plague patients. These issues make accurate detection of patients and the development of clinical case definitions and triage algorithms in urban pneumonic plague outbreaks difficult.
Author Lovering, Andrew
Razafimandimby, Dominique
Randremanana, Rindra
Hasiniatsy, Rodrigue N. E.
Raberahona, Mihaja
Rajerison, Minoarisoa
Rakotomalala, Rado
Horby, Peter
Razanajatovo, Norosoa
Castle, Lyndsey
Frédérique, Randrianirina
Razafinambinintsoa, Tiana
Heraud, Jean-Michel
Renaud, Bertrand
Mangahasimbola, Reziky T.
Andrianaivoarimanana, Voahangy
Andrianarintsiferantsoa, Faraniaina
Baril, Laurence
Funk, Anna
Read, Liam
Fontanet, Arnaud
Randria, Mamy
Andriantsalama, Prisca
Salam, Alex P.
Bertherat, Eric
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Financial support: This study was funded by the United Kingdom Public Health Rapid Support Team.
Authors’ addresses: Alex P. Salam, Lyndsey Castle, and Peter Horby, University of Oxford, Oxford, United Kingdom, E-mails: alex.salam@ndm.ox.ac.uk, lyndsey.castle@ndm.ox.ac.uk, and peter.horby@ndm.ox.ac.uk. Mihaja Raberahona, Tiana Razafinambinintsoa, Rado Rakotomalala, and Mamy Randria, Centre Hospitalier Befelatanana, Antananarivo, Madagascar, E-mails: raberahona@gmail.com, jdnambinintsoa@gmail.com, rakotomalalaradodhunant@gmail.com, and rmamyjeandedieu@yahoo.fr. Prisca Andriantsalama, Reziky T. Mangahasimbola, Jean-Michel Heraud, Voahangy Andrianaivoarimanana, Randrianirina Frédérique, Norosoa Razanajatovo, Laurence Baril, Minoarisoa Rajerison, and Rindra Randremanana, Institut Pasteur de Madagascar, Antananarivo, Madagascar, E-mails: pandriatsalama@pasteur.mg, mreziky@pasteur.mg, jmheraud@pasteur.mg, kekely@pasteur.mg, frederique@pasteur.mg, norosoa@pasteur.mg, lbaril@pasteur.mg, mino@pasteur.mg, and rrandrem@pasteur.mg. Liam Read and Andrew Lovering, North Bristol NHS trust, Bristol, United Kingdom, E-mails: liam.read@nbt.nhs.uk and andrew.lovering@nbt.nhs.uk. Faraniaina Andrianarintsiferantsoa, Centre Hospitalier Anti-Pesteux d’Ambohimiandra, Antananarivo, Madagascar, E-mail: drfaraniaina@gmail.com. Rodrigue N. E. Hasiniatsy and Dominique Razafimandimby, Centre Hospitalier de Soavinandriana, Antananarivo, Madagascar, E-mails: hasiniatsy.rodrigue@yahoo.fr and d.razafimandimby@yahoo.fr. Anna Funk and Arnaud Fontanet, Institut Pasteur Paris, Paris, France, E-mails: anna-louise.funk@pasteur.fr and arnaud.fontanet@pasteur.fr. Bertrand Renaud, Université Paris Descartes, Paris, France, E-mail: bertrand.renaud@parisdescartes.fr. Eric Bertherat, World Health Organization, Geneva, Switzerland, E-mail: bertherate@who.int.
These authors contributed equally to this work.
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Snippet In late 2017, Madagascar experienced a large urban outbreak of pneumonic plague, the largest outbreak to date this century. During the outbreak, there were...
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SubjectTerms Adolescent
Adult
Aged
Antibiotics
Bacterial infections
Biochemistry, Molecular Biology
Child
Child, Preschool
Cohort analysis
Cohort Studies
Emerging diseases
Epidemics
Female
Human health and pathology
Humans
Infant
Infectious diseases
Life Sciences
Madagascar
Madagascar - epidemiology
Male
Medical diagnosis
Microbiology and Parasitology
Middle Aged
Molecular biology
Patients
Plague
Plague - epidemiology
Plague - pathology
Prospective Studies
Santé publique et épidémiologie
Virology
Title Factors Influencing Atypical Clinical Presentations during the 2017 Madagascar Pneumonic Plague Outbreak: A Prospective Cohort Study
URI https://www.ncbi.nlm.nih.gov/pubmed/32274983
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https://pasteur.hal.science/pasteur-03250581
https://pubmed.ncbi.nlm.nih.gov/PMC7253123
Volume 102
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